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N-(3-chlorophenyl)-2-iodoacetamide

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Identification
Molecular formula
C8H7ClINO
CAS number
1635-61-6
IUPAC name
N-(3-chlorophenyl)-2-iodo-acetamide
State
State

At room temperature, N-(3-chlorophenyl)-2-iodoacetamide is in a solid state. It exists as crystalline solid under normal conditions.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
311.49g/mol
Molar mass
311.4870g/mol
Density
2.0650g/cm3
Appearence

N-(3-chlorophenyl)-2-iodoacetamide is typically a crystalline solid under standard conditions. It may appear as a solid with characteristic crystalline features depending on the purification and crystallization process used.

Comment on solubility

Solubility of N-(3-chlorophenyl)-2-iodo-acetamide

N-(3-chlorophenyl)-2-iodo-acetamide, a compound with a notable structure, showcases interesting solubility characteristics that are worth exploring. The solubility of this compound is influenced by various factors, including:

  • Polarity: The presence of polar functional groups in its molecular structure can enhance solubility in polar solvents, such as water.
  • Hydrogen bonding: This compound may form hydrogen bonds with solvents, particularly if soluble in protic solvents.
  • Substituent Effects: The 3-chlorophenyl group and the iodine atom introduce steric and electronic effects that can significantly affect solubility.
  • Temperature: Like many organic compounds, solubility can increase with temperature; thus, understanding the specific solubility curve is essential.

Moreover, it can be stated that:

“A compound’s solubility is often a reflection of the interactions between solute and solvent at the molecular level.”

In conclusion, the solubility of N-(3-chlorophenyl)-2-iodo-acetamide can be described as moderate to low in water, typical for many substituted amides, while highlighting its behavior in organic solvents where it could exhibit a different solubility profile. Overall, the understanding of its solubility is fundamental for its applications in chemical processes and formulations.

Interesting facts

Interesting Facts about N-(3-chlorophenyl)-2-iodo-acetamide

N-(3-chlorophenyl)-2-iodo-acetamide is a fascinating chemical compound with notable features that pique the interest of both researchers and students in the field of chemistry. Here are some intriguing aspects of this compound:

  • Structure and Functionality: The compound features a chlorophenyl group and an iodo-acetamide moiety, combining elements of both aromatic chemistry and halogen chemistry, which gives it unique reactivity and properties.
  • Applications: Its unique structure makes it a candidate for various applications, including:
    • Pharmaceutical development, particularly in targeting specific biological pathways.
    • Organic synthesis, where it can serve as an intermediate in the creation of more complex molecules.
  • Research Interest: The presence of both iodine and chlorine atoms in its structure can lead to interesting studies on reactivity, especially in nucleophilic substitution reactions.
  • Toxicity Considerations: Compounds containing halogens often require careful handling due to potential toxicity. This emphasizes the importance of safety protocols in the laboratory.

In summary, N-(3-chlorophenyl)-2-iodo-acetamide is more than just a simple chemical formula. It embodies the complexity of chemical interactions and the potential for innovative applications in modern science. As one researcher put it, "The true beauty of chemistry lies in the unexpected connections between seemingly simple molecules."

Synonyms
17641-03-1
ACETANILIDE, 3'-CHLORO-2-IODO-
3'-Chloro-2-iodoacetanilide
BRN 2831842
DTXSID50170126
DTXCID0092617
N-(3-chlorophenyl)-2-iodoacetamide
ACETANILIDE,3-CHLORO-2-IODO-
AKOS003107425
n-(3-chloro-phenyl)-2-iodo-acetamide